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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 11-77211170-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=77211170&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 77211170,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000409709.9",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6070C>A",
          "hgvs_p": "p.Arg2024Arg",
          "transcript": "NM_000260.4",
          "protein_id": "NP_000251.3",
          "transcript_support_level": null,
          "aa_start": 2024,
          "aa_end": null,
          "aa_length": 2215,
          "cds_start": 6070,
          "cds_end": null,
          "cds_length": 6648,
          "cdna_start": 6360,
          "cdna_end": null,
          "cdna_length": 7483,
          "mane_select": "ENST00000409709.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6070C>A",
          "hgvs_p": "p.Arg2024Arg",
          "transcript": "ENST00000409709.9",
          "protein_id": "ENSP00000386331.3",
          "transcript_support_level": 1,
          "aa_start": 2024,
          "aa_end": null,
          "aa_length": 2215,
          "cds_start": 6070,
          "cds_end": null,
          "cds_length": 6648,
          "cdna_start": 6360,
          "cdna_end": null,
          "cdna_length": 7483,
          "mane_select": "NM_000260.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.5956C>A",
          "hgvs_p": "p.Arg1986Arg",
          "transcript": "ENST00000458637.6",
          "protein_id": "ENSP00000392185.2",
          "transcript_support_level": 1,
          "aa_start": 1986,
          "aa_end": null,
          "aa_length": 2175,
          "cds_start": 5956,
          "cds_end": null,
          "cds_length": 6528,
          "cdna_start": 6222,
          "cdna_end": null,
          "cdna_length": 7336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 50,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.5923C>A",
          "hgvs_p": "p.Arg1975Arg",
          "transcript": "ENST00000409619.6",
          "protein_id": "ENSP00000386635.2",
          "transcript_support_level": 1,
          "aa_start": 1975,
          "aa_end": null,
          "aa_length": 2166,
          "cds_start": 5923,
          "cds_end": null,
          "cds_length": 6501,
          "cdna_start": 6270,
          "cdna_end": null,
          "cdna_length": 7106,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.3496C>A",
          "hgvs_p": "p.Arg1166Arg",
          "transcript": "ENST00000458169.2",
          "protein_id": "ENSP00000417017.2",
          "transcript_support_level": 1,
          "aa_start": 1166,
          "aa_end": null,
          "aa_length": 1357,
          "cds_start": 3496,
          "cds_end": null,
          "cds_length": 4074,
          "cdna_start": 3496,
          "cdna_end": null,
          "cdna_length": 4616,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "n.*642C>A",
          "hgvs_p": null,
          "transcript": "ENST00000670577.1",
          "protein_id": "ENSP00000499323.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4966,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "n.*642C>A",
          "hgvs_p": null,
          "transcript": "ENST00000670577.1",
          "protein_id": "ENSP00000499323.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4966,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 44,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6134C>A",
          "hgvs_p": "p.Pro2045Gln",
          "transcript": "XM_047426972.1",
          "protein_id": "XP_047282928.1",
          "transcript_support_level": null,
          "aa_start": 2045,
          "aa_end": null,
          "aa_length": 2095,
          "cds_start": 6134,
          "cds_end": null,
          "cds_length": 6288,
          "cdna_start": 6231,
          "cdna_end": null,
          "cdna_length": 6398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.5956C>A",
          "hgvs_p": "p.Arg1986Arg",
          "transcript": "NM_001127180.2",
          "protein_id": "NP_001120652.1",
          "transcript_support_level": null,
          "aa_start": 1986,
          "aa_end": null,
          "aa_length": 2175,
          "cds_start": 5956,
          "cds_end": null,
          "cds_length": 6528,
          "cdna_start": 6246,
          "cdna_end": null,
          "cdna_length": 7363,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 50,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.5923C>A",
          "hgvs_p": "p.Arg1975Arg",
          "transcript": "NM_001369365.1",
          "protein_id": "NP_001356294.1",
          "transcript_support_level": null,
          "aa_start": 1975,
          "aa_end": null,
          "aa_length": 2166,
          "cds_start": 5923,
          "cds_end": null,
          "cds_length": 6501,
          "cdna_start": 6326,
          "cdna_end": null,
          "cdna_length": 7449,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6160C>A",
          "hgvs_p": "p.Arg2054Arg",
          "transcript": "XM_011545046.3",
          "protein_id": "XP_011543348.2",
          "transcript_support_level": null,
          "aa_start": 2054,
          "aa_end": null,
          "aa_length": 2258,
          "cds_start": 6160,
          "cds_end": null,
          "cds_length": 6777,
          "cdna_start": 6257,
          "cdna_end": null,
          "cdna_length": 7190,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6154C>A",
          "hgvs_p": "p.Arg2052Arg",
          "transcript": "XM_017017778.2",
          "protein_id": "XP_016873267.1",
          "transcript_support_level": null,
          "aa_start": 2052,
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          "aa_length": 2256,
          "cds_start": 6154,
          "cds_end": null,
          "cds_length": 6771,
          "cdna_start": 6251,
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          "cdna_length": 7184,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6151C>A",
          "hgvs_p": "p.Arg2051Arg",
          "transcript": "XM_017017779.2",
          "protein_id": "XP_016873268.1",
          "transcript_support_level": null,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2255,
          "cds_start": 6151,
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          "cds_length": 6768,
          "cdna_start": 6248,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6160C>A",
          "hgvs_p": "p.Arg2054Arg",
          "transcript": "XM_017017780.2",
          "protein_id": "XP_016873269.1",
          "transcript_support_level": null,
          "aa_start": 2054,
          "aa_end": null,
          "aa_length": 2245,
          "cds_start": 6160,
          "cds_end": null,
          "cds_length": 6738,
          "cdna_start": 6257,
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          "cdna_length": 7380,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 45,
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          "intron_rank": null,
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          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6070C>A",
          "hgvs_p": "p.Arg2024Arg",
          "transcript": "XM_011545044.3",
          "protein_id": "XP_011543346.1",
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          "aa_start": 2024,
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          "aa_length": 2228,
          "cds_start": 6070,
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          "cds_length": 6687,
          "cdna_start": 6360,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6064C>A",
          "hgvs_p": "p.Arg2022Arg",
          "transcript": "XM_017017781.2",
          "protein_id": "XP_016873270.1",
          "transcript_support_level": null,
          "aa_start": 2022,
          "aa_end": null,
          "aa_length": 2226,
          "cds_start": 6064,
          "cds_end": null,
          "cds_length": 6681,
          "cdna_start": 6161,
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          "cdna_length": 7094,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6046C>A",
          "hgvs_p": "p.Arg2016Arg",
          "transcript": "XM_017017782.2",
          "protein_id": "XP_016873271.1",
          "transcript_support_level": null,
          "aa_start": 2016,
          "aa_end": null,
          "aa_length": 2220,
          "cds_start": 6046,
          "cds_end": null,
          "cds_length": 6663,
          "cdna_start": 6143,
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          "cdna_length": 7075,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
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          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6043C>A",
          "hgvs_p": "p.Arg2015Arg",
          "transcript": "XM_017017783.2",
          "protein_id": "XP_016873272.1",
          "transcript_support_level": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
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          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6037C>A",
          "hgvs_p": "p.Arg2013Arg",
          "transcript": "XM_047426973.1",
          "protein_id": "XP_047282929.1",
          "transcript_support_level": null,
          "aa_start": 2013,
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          "cds_start": 6037,
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          "cdna_start": 6144,
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          "cdna_length": 7077,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MYO7A",
          "gene_hgnc_id": 7606,
          "hgvs_c": "c.6046C>A",
          "hgvs_p": "p.Arg2016Arg",
          "transcript": "XM_017017788.2",
          "protein_id": "XP_016873277.1",
          "transcript_support_level": null,
          "aa_start": 2016,
          "aa_end": null,
          "aa_length": 2207,
          "cds_start": 6046,
          "cds_end": null,
          "cds_length": 6624,
          "cdna_start": 6143,
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          "cdna_length": 7266,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
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      "gene_symbol": "MYO7A",
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      "dbsnp": "rs111033198",
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      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": 0,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 0,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.15000000596046448,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.15,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.452,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
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      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
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      "acmg_score": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4,BP7",
      "acmg_by_gene": [
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          "pathogenic_score": 2,
          "criteria": [
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            "BP4",
            "BP7"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000409709.9",
          "gene_symbol": "MYO7A",
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          "hgvs_c": "c.6070C>A",
          "hgvs_p": "p.Arg2024Arg"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}